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Acetic acid 2-ethylallyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55670-09-2

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55670-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55670-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,7 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55670-09:
(7*5)+(6*5)+(5*6)+(4*7)+(3*0)+(2*0)+(1*9)=132
132 % 10 = 2
So 55670-09-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-4-6(2)5-9-7(3)8/h2,4-5H2,1,3H3

55670-09-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylidenebutyl acetate

1.2 Other means of identification

Product number -
Other names Acetic acid 2-ethylallyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:55670-09-2 SDS

55670-09-2Relevant academic research and scientific papers

Cross-metathesis reactions of homoallyl methyl malonates with sterically hindered allylic esters

Barile, Fabio,Bassetti, Mauro,D'Annibale, Andrea,Gerometta, Renzo,Palazzi, Michele

experimental part, p. 6519 - 6526 (2011/12/05)

The methyl malonate esters of 3-buten-1-ol and 2-methyl-3-buten-1-ol can be coupled efficiently to different methallylic esters in the presence of the second-generation Grubbs catalyst to yield trisubstituted olefins by the cross-metathesis reaction. Product selectivity and yields depend on the relative amounts of reagents and to a minor extent on the methallylic ester functional group. Alkyl substituents at either the allylic or the geminal positions significantly affect the product yields and the E/Z stereoselectivity. The cross-metathesis reactions of homoallyl malonates with allylic esters featuring a variety of alkyl substituents at the vinylic and/or allylic positions afford trisubstituted olefins. Copyright

Regioselective Synthesis of Hydroxy Sulphides via Trifluoroacetoxysulphenylation of Derivatives of Allylic Alcohols

Samii, Zakaria K. M. Abd El,Ashmawy, Mohamed I. Al,Mellor, John M.

, p. 2509 - 2516 (2007/10/02)

Reaction of manganese(III) acetate with diphenyl disulphide in dichloromethane-trifluoroacetic acid in the presence of allylic esters gives trifluoroacetoxy sulphides, which on hydrolysis readily afford vicinal hydroxy sulphides.With acetate esters, neighbouring group participation by the acetate functionality controls the reaction course.Thus regiospecific addition to allyl acetate affords after hydrolysis only 3-phenylthiopropane-1,2-diol.In contrast, with trifluoroacetate esters the inductive effects of the trifluoroacetate functionality lead to a different regiocontrol.Thus addition of diphenyl disulphide to allyl trifluoroacetate gives after hydrolysis only 2-phenylthiopropane-1,3-diol.The regio- and stereochemistry of addition to a variety of other allylic (and homoallylic) esters is described and the extension of this type of regiocontrol is discussed.

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